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农杆菌介导的 egfp-hph 融合基因在 gpd 启动子控制下在糙皮侧耳中的表达。

Agrobacterium tumefaciens mediated fused egfp-hph gene expression under the control of gpd promoter in Pleurotus ostreatus.

机构信息

College of Food Science and Technology, Huazhong Agricultural University, 1 Lion Hill Road, Wuhan 430070, China.

出版信息

Microbiol Res. 2011 May 20;166(4):314-22. doi: 10.1016/j.micres.2010.07.001. Epub 2010 Sep 23.

Abstract

A transformation system for the basidiomycete Pleurotus ostreatus was established using agrobacterium-mediated infection. Following P. ostreatus glyceraldehyde-3-phosphate dehydrogenase gene analysis, its promoter region including two introns was used as cis-regulatory element to drive expression of enhanced green fluorescent protein (eGFP). As a selection marker, the hygromycin phosphotransferase (hph) gene cassette was used in the binary vector pPEH. Mycelia without pretreatment were found to be the most efficient recipients in transformation experiments while fruiting body tissue or basidiospores showed lower transformation rates. A transformation efficiency of 75% was achieved. After subculturing, putative transformants were screened by PCR and Southern blot analysis showing the expected ectopic integration of the transforming DNA. At the same time, the promotor region was shown to drive expression of selection marker as well as eGFP that could be visualized, which will be helpful for future investigation using Agrobacterium tumefaciens mediated transformation for functional characterization of genes in the mushroom forming basidioymcete P. ostreatus.

摘要

利用根癌农杆菌介导的感染,建立了一种用于担子菌糙皮侧耳(Pleurotus ostreatus)的转化系统。在分析糙皮侧耳甘油醛-3-磷酸脱氢酶基因后,我们将其启动子区域(包含两个内含子)用作顺式调控元件,以驱动增强型绿色荧光蛋白(eGFP)的表达。作为选择标记,潮霉素磷酸转移酶(hph)基因盒被用于双元载体 pPEH。在转化实验中,未经预处理的菌丝体被发现是最有效的受体,而子实体组织或担孢子的转化效率较低。我们实现了 75%的转化效率。继代培养后,通过 PCR 和 Southern blot 分析筛选出了预期的转化 DNA 的异位整合的假转化体。同时,启动子区域被证明可以驱动选择标记和 eGFP 的表达,这些可以被可视化,这将有助于利用根癌农杆菌介导的转化对形成蘑菇的担子菌糙皮侧耳中的基因进行功能表征的未来研究。

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